International safety notice
Urgent Field Safety Notice for BritePro Solo Single Use Fibre Optic Laryngoscope by Flexicare Medical Limited
Germany / BfArM · DEU · Dec 4, 2019
Key facts
| Title | Urgent Field Safety Notice for BritePro Solo Single Use Fibre Optic Laryngoscope by Flexicare Medical Limited |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | BritePro Solo Single Use Fibre Optic Laryngoscope |
| Manufacturer | Flexicare Medical Limited |
| Models | 040-333, 2019-001, 040-342, QA079, 040‐342, 180900401, 190100335, 2019‐001, 040‐333 |
| Date | Dec 4, 2019 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1